Publications of Uz, E.
2010
| , , , , , , , , and , Analysis of skewed X-chromosome inactivation in females with rheumatoid arthritis and autoimmune thyroid diseases (2010), in: Arthritis & Rheumatism, 11(106-1--8) |
| , , , , , , , and , Increased frequency of extremely skewed X chromosome inactivation in juvenile idiopathic arthritis (2010), in: Arthritis & Rheumatism, 60(3410-3412) |
2009
| , , , , , and , Extreme clonality in lymphoblastoid cell lines with implications for allele specific expression analyses (2009), in: Plos One, 3(2966) |
| , , , , , , and , Mutations in the very low-density lipoprotein receptor VLDLR cause cerebellar hypoplasia and quadrupedal locomotion in humans (2009), in: Proceedings of National Academy of Sciences USA, 105(4232-4236) |
| , , , , , , and , Reply to Herz et al. And Humprey et al.: Genetic heterogeneity of cerebellar hypoplasia with quadruprdal locomotion (2009), in: Proceedings of National Academy of Sciences USA, 105(32-33) |
| , , , , , and , Skewed X-chromosome inactivation in scleroderma (2009), in: Clinical Reviews in Allergy & Immunology |
2008
| , , , , , , , , and , Skewed X-inactivation in an X-linked Nystagmus Family Resulted From a Novel, p.R229G, Missence Mutation in the FRMD7 Gene (2008), in: British J of Ophthalmology, 92(135-141) |
2007
| , , , , , , , and , Evidence from autoimmune thyroiditis of skewed X-chromosome inactivation in female predisposition to autoimmunity (2007), in: European J of Human Genetics, 14(791-797) |
| , , and , Extremely skewed X-chromosome inactivation in pre-eclampsia (2007), in: Human Genetics, 121(101-105) |